Concepts (107)
Concepts are derived automatically from a person's publications.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
| Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
|---|
| Myocardium | 9 | 2017 | 251 | 1.580 |
Why?
|
| Cytoskeleton | 13 | 2017 | 111 | 1.400 |
Why?
|
| Carrier Proteins | 7 | 2017 | 318 | 1.260 |
Why?
|
| Myosins | 15 | 2014 | 35 | 1.060 |
Why?
|
| Cardiac Myosins | 3 | 2017 | 7 | 0.880 |
Why?
|
| Actins | 6 | 2017 | 162 | 0.820 |
Why?
|
| Muscles | 17 | 2002 | 84 | 0.740 |
Why?
|
| Phosphorylation | 6 | 2017 | 973 | 0.480 |
Why?
|
| Heart | 1 | 2017 | 181 | 0.470 |
Why?
|
| Image Processing, Computer-Assisted | 7 | 2010 | 170 | 0.400 |
Why?
|
| Zebrafish | 1 | 2014 | 146 | 0.390 |
Why?
|
| Fourier Analysis | 6 | 2014 | 45 | 0.290 |
Why?
|
| Animals | 36 | 2017 | 16695 | 0.290 |
Why?
|
| Horseshoe Crabs | 12 | 1995 | 15 | 0.270 |
Why?
|
| Protein Binding | 5 | 2017 | 1076 | 0.270 |
Why?
|
| Microscopy, Electron | 19 | 2012 | 209 | 0.260 |
Why?
|
| Rabbits | 9 | 2009 | 292 | 0.250 |
Why?
|
| Models, Molecular | 6 | 2015 | 875 | 0.230 |
Why?
|
| Actomyosin | 2 | 1995 | 7 | 0.220 |
Why?
|
| Sarcomeres | 2 | 2015 | 8 | 0.200 |
Why?
|
| Imaging, Three-Dimensional | 4 | 2014 | 89 | 0.200 |
Why?
|
| Temperature | 2 | 1995 | 314 | 0.200 |
Why?
|
| Goldfish | 5 | 2010 | 18 | 0.160 |
Why?
|
| Tropomyosin | 4 | 2015 | 16 | 0.160 |
Why?
|
| Staining and Labeling | 6 | 2005 | 106 | 0.160 |
Why?
|
| Mice | 5 | 2017 | 6490 | 0.150 |
Why?
|
| X-Ray Diffraction | 10 | 2006 | 66 | 0.130 |
Why?
|
| Cyclic AMP-Dependent Protein Kinases | 1 | 2017 | 74 | 0.130 |
Why?
|
| Cattle | 3 | 2015 | 505 | 0.120 |
Why?
|
| Myofibrils | 3 | 2012 | 12 | 0.120 |
Why?
|
| Kinetics | 1 | 2017 | 698 | 0.120 |
Why?
|
| Mice, Inbred BALB C | 1 | 2017 | 686 | 0.110 |
Why?
|
| Mice, Transgenic | 1 | 2017 | 658 | 0.110 |
Why?
|
| Osmolar Concentration | 1 | 1994 | 53 | 0.110 |
Why?
|
| Fishes | 2 | 2006 | 59 | 0.090 |
Why?
|
| Fish Proteins | 1 | 2010 | 14 | 0.080 |
Why?
|
| Microscopy, Electron, Scanning | 1 | 2010 | 158 | 0.080 |
Why?
|
| Protein Structure, Secondary | 2 | 2007 | 185 | 0.080 |
Why?
|
| Cyprinidae | 1 | 1989 | 10 | 0.080 |
Why?
|
| Scorpions | 3 | 1985 | 7 | 0.080 |
Why?
|
| Bivalvia | 1 | 1989 | 25 | 0.080 |
Why?
|
| Troponin | 1 | 2009 | 17 | 0.080 |
Why?
|
| Cysteine | 1 | 1989 | 101 | 0.070 |
Why?
|
| Organometallic Compounds | 2 | 1985 | 72 | 0.070 |
Why?
|
| Cardiomyopathy, Hypertrophic, Familial | 1 | 2007 | 1 | 0.070 |
Why?
|
| Species Specificity | 5 | 1994 | 279 | 0.070 |
Why?
|
| Muscle, Skeletal | 3 | 2010 | 308 | 0.070 |
Why?
|
| Myosin-Light-Chain Kinase | 3 | 1996 | 8 | 0.060 |
Why?
|
| Mice, Knockout | 1 | 2007 | 1010 | 0.050 |
Why?
|
| Chickens | 2 | 2015 | 148 | 0.050 |
Why?
|
| Protein Conformation | 3 | 2010 | 420 | 0.050 |
Why?
|
| Computers | 5 | 1986 | 35 | 0.050 |
Why?
|
| Octoxynol | 1 | 2002 | 19 | 0.050 |
Why?
|
| Detergents | 1 | 2002 | 25 | 0.050 |
Why?
|
| Rana pipiens | 3 | 1986 | 62 | 0.040 |
Why?
|
| Crystallography, X-Ray | 2 | 2012 | 285 | 0.040 |
Why?
|
| Software | 1 | 2002 | 234 | 0.040 |
Why?
|
| Macromolecular Substances | 4 | 1995 | 95 | 0.040 |
Why?
|
| Spiders | 4 | 1995 | 9 | 0.040 |
Why?
|
| Calcium | 3 | 2015 | 487 | 0.040 |
Why?
|
| Muscle Relaxation | 2 | 1995 | 19 | 0.030 |
Why?
|
| Binding Sites | 2 | 2009 | 670 | 0.030 |
Why?
|
| Male | 1 | 2017 | 22779 | 0.030 |
Why?
|
| Myosin Light Chains | 1 | 1996 | 6 | 0.030 |
Why?
|
| Female | 1 | 2017 | 24018 | 0.030 |
Why?
|
| Muscle Fibers, Skeletal | 1 | 1996 | 70 | 0.030 |
Why?
|
| Cardiomyopathy, Hypertrophic | 1 | 2015 | 24 | 0.030 |
Why?
|
| Amino Acid Substitution | 1 | 2015 | 135 | 0.030 |
Why?
|
| Negative Staining | 1 | 1995 | 1 | 0.030 |
Why?
|
| Protein Structure, Tertiary | 2 | 2009 | 427 | 0.030 |
Why?
|
| Psoas Muscles | 1 | 1994 | 1 | 0.030 |
Why?
|
| Recombinant Proteins | 1 | 2015 | 522 | 0.030 |
Why?
|
| Ranidae | 1 | 1993 | 12 | 0.030 |
Why?
|
| Platinum | 1 | 1993 | 23 | 0.030 |
Why?
|
| Amino Acid Sequence | 1 | 2015 | 1188 | 0.020 |
Why?
|
| Models, Biological | 3 | 2002 | 711 | 0.020 |
Why?
|
| Molecular Sequence Data | 1 | 2015 | 1559 | 0.020 |
Why?
|
| Muscle Proteins | 1 | 2012 | 52 | 0.020 |
Why?
|
| Protein Kinases | 1 | 2012 | 100 | 0.020 |
Why?
|
| Mutation | 1 | 2015 | 1169 | 0.020 |
Why?
|
| Gene Expression Regulation | 1 | 2015 | 1066 | 0.020 |
Why?
|
| Microscopy, Electron, Transmission | 1 | 2010 | 160 | 0.020 |
Why?
|
| Avidin | 1 | 1989 | 4 | 0.020 |
Why?
|
| Protein Multimerization | 1 | 2010 | 114 | 0.020 |
Why?
|
| NADH Tetrazolium Reductase | 1 | 1989 | 1 | 0.020 |
Why?
|
| NADH, NADPH Oxidoreductases | 1 | 1989 | 12 | 0.020 |
Why?
|
| Amino Acid Motifs | 1 | 2009 | 94 | 0.020 |
Why?
|
| Vanadates | 1 | 1988 | 8 | 0.020 |
Why?
|
| Electron Probe Microanalysis | 2 | 1985 | 13 | 0.020 |
Why?
|
| Potassium Chloride | 1 | 1988 | 26 | 0.020 |
Why?
|
| Cross-Linking Reagents | 1 | 1988 | 51 | 0.020 |
Why?
|
| Uranium | 2 | 1985 | 23 | 0.020 |
Why?
|
| Optics and Photonics | 3 | 1983 | 43 | 0.020 |
Why?
|
| Adenosine Triphosphate | 1 | 1988 | 205 | 0.020 |
Why?
|
| Signal Transduction | 1 | 2015 | 2111 | 0.020 |
Why?
|
| Models, Structural | 1 | 1986 | 12 | 0.020 |
Why?
|
| Hydrolyzable Tannins | 1 | 1985 | 20 | 0.010 |
Why?
|
| Muscle Contraction | 1 | 1985 | 67 | 0.010 |
Why?
|
| Models, Chemical | 1 | 1982 | 205 | 0.010 |
Why?
|
| Humans | 2 | 2015 | 42163 | 0.010 |
Why?
|
| Computer Simulation | 1 | 2002 | 404 | 0.010 |
Why?
|
| Serum Albumin, Bovine | 1 | 1996 | 49 | 0.010 |
Why?
|
| Biophysical Phenomena | 1 | 1995 | 22 | 0.010 |
Why?
|
| Biophysics | 1 | 1995 | 38 | 0.010 |
Why?
|
| Calmodulin | 1 | 1991 | 44 | 0.010 |
Why?
|
| Histocytochemistry | 1 | 1989 | 47 | 0.000 |
Why?
|
| Electrophoresis, Polyacrylamide Gel | 1 | 1983 | 198 | 0.000 |
Why?
|